HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94762804delinsTACCCT , CM000672.2:g.94762804delinsTACCCT | GRCh38 |
NG_008384.2:g.5099delinsTACCCT | |
NG_008384.3:g.5124delinsTACCCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.99delinsTACCCT MANE Select | ENSP00000360372.3:p.Pro35LeufsTer6 | |
ENST00000371321.7:c.99delinsTACCCT | ENSP00000360372.3:p.Pro35LeufsTer6 | |
ENST00000464755.1:c.932-12254delinsTACCCT | ENSP00000483243.1:n.932-12254delinsTACCCT | |
ENST00000480405.2:c.99delinsTACCCT | ENSP00000483847.1:p.Pro35LeufsTer6 | |
NM_000769.2:c.99delinsTACCCT | NP_000760.1:p.Pro35LeufsTer6 | |
NM_000769.4:c.99delinsTACCCT MANE Select | NP_000760.1:p.Pro35LeufsTer6 |